http://jcb.sagepub.com/content/36/2/283.full
- 1Research Imaging Institute, University of Texas Health Science Center, San Antonio, TX, USA
- 2Department of Ophthalmology, University of Texas Health Science Center, San Antonio, TX, USA
- 3Department of Radiology, University of Texas Health Science Center, San Antonio, TX, USA
- 4South Texas Veterans Health Care System, Department of Veterans Affairs, San Antonio, TX, USA
- Qiang Shen, Research Imaging Institute, University of Texas Health Science Center at San Antonio, 8403 Floyd Curl Dr, San Antonio, TX 78229, USA. Email: shenq3@uthscsa.edu Timothy Q Duong, Research Imaging Institute, University of Texas Health Science Center at San Antonio, 8403 Floyd Curl Dr, San Antonio, TX 78229, USA. Email: duongt@uthscsa.edu
Abstract
T2*-weighted MRI of
transient oxygen challenge (OC) showed exaggerated OC percent changes in
the ischemic tissue at risk compared
to normal tissue. One ambiguity is that regions
with high vascular density also showed exaggerated OC percent changes.
This
study explored time-to-peak (TTP) of the OC percent
changes to improve the utility of T2*-weighted OC
MRI. Experiments were performed longitudinally at 30 min, 150 min and
24 h after transient (60-min) stroke in
rats. Ischemic core, normal, and mismatch tissue
were classified pixel-by-pixel based on apparent diffusion coefficient
and
cerebral blood flow. Major findings were: (i)
Delayed OC TTP was localized to and corresponded well with the
perfusion-diffusion
mismatch. (ii) By contrast, the exaggerated OC
percent changes were less localized, with changes not only in the
at-risk tissue
but also in some areas of the contralesional
hemisphere with venous vessel origins. (iii) The OC time-course of the
mismatch
tissue was biphasic, with a faster initial increase
followed by a slower increase. (iv) At-risk tissue with delayed TTP and
exaggerated OC was normal after reperfusion and the
at-risk tissue was mostly (83 ± 18%) rescued by reperfusion as
indicated
by normal 24-h T2. OC TTP offers unique information toward better characterization of at-risk tissue in ischemic stroke.
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